Canonical Allele Identifier: CA400683979
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224293A>C (hg19) chr17:g.66228175A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228175A>C , CM000679.2:g.66228175A>C GRCh38
NC_000017.10:g.64224293A>C , CM000679.1:g.64224293A>C GRCh37
NC_000017.9:g.61654755A>C NCBI36
NG_012045.1:g.6264T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.86T>G MANE Select ENSP00000205948.6:p.Leu29Ter
ENST00000205948.10:c.86T>G ENSP00000205948.6:p.Leu29Ter
ENST00000577982.1:c.86T>G ENSP00000464301.1:p.Leu29Ter
ENST00000581797.5:c.-95T>G ENSP00000463553.1:n.-95T>G
NM_000042.2:c.86T>G NP_000033.2:p.Leu29Ter
NM_000042.3:c.86T>G MANE Select NP_000033.2:p.Leu29Ter
Search 100 bp 5'
Search 100 bp 3'